A novel and efficient route to (E)-alk-1-enyl boronic acid derivatives from (E)-1-(trimethylsilyl)alk-1-enes and a formal Suzuki–Miyaura cross-coupling reaction starting with vinylsilanes

Gianluca M. Farinola; Vito Fiandanese; Luigia Mazzone; Francesco Naso

doi:10.1039/C39950002523

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Journal of the Chemical Society, Chemical Communications

Issue 24, 1995

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A novel and efficient route to (E)-alk-1-enyl boronic acid derivatives from (E)-1-(trimethylsilyl)alk-1-enes and a formal Suzuki–Miyaura cross-coupling reaction starting with vinylsilanes

Gianluca M. Farinola , Vito Fiandanese , Luigia Mazzone and Francesco Naso

J. Chem. Soc., Chem. Commun., 1995, 2523-2524

DOI: 10.1039/C39950002523

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A novel and highly efficient conversion of vinylsilanes into vinyl boronates is described together with their Suzuki–Miyaura cross-coupling reaction, performed without isolating the intermediate resulting from borodesllyiation.

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Journal of the Chemical Society, Chemical Communications

A novel and efficient route to (E)-alk-1-enyl boronic acid derivatives from (E)-1-(trimethylsilyl)alk-1-enes and a formal Suzuki–Miyaura cross-coupling reaction starting with vinylsilanes

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